Near-field scanning optical microscopy in liquid for high resolution single molecule detection on dendritic cells

被引:81
作者
Koopman, M
Cambi, A
de Bakker, BI
Joosten, B
Figdor, CG
van Hulst, NF
Garcia-Parajo, MF
机构
[1] Univ Twente, Fac Sci & Technol, Appl Opt Grp, NL-7500 AE Enschede, Netherlands
[2] Univ Twente, MESA Inst Nanotechnol, NL-7500 AE Enschede, Netherlands
[3] Univ Nijmegen, Med Ctr, Nijmegen Ctr Mol Life Sci, Dept Tumor Immunol, Nijmegen, Netherlands
关键词
near-field scanning optical microscopy; single molecule detection; sub-diffraction limit; cell surface distribution; microdomain; DC-SIGN;
D O I
10.1016/j.febslet.2004.07.035
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Clustering of cell surface receptors into microdomains in the plasma membrane is an important mechanism for regulating cellular functions. Unfortunately, these domains are often too small to be resolved with conventional optical microscopy. Near-field scanning optical microscopy (NSOM) is a relatively new technique that combines ultra high optical resolution, down to 70 nm, with single molecule detection sensitivity. As such, the technique holds great potential for direct visualisation of domains at the cell surface. Yet, NSOM operation under liquid conditions is far from trivial. In this contribution, we show that the performance of NSOM can be extended to measurements in liquid environments using a diving bell concept. For the first time, individual fluorescent molecules on the membrane of cells in solution are imaged with a spatial resolution of 90 nm. Furthermore, using this technique we have been able to directly visualise nanometric sized domains of the C-type lectin DC-SIGN on the membrane of dendritic cells, both in air and in liquid. (C) 2004 Published by Elsevier B.V. on behalf of the Federation of European Biochemical Societies.
引用
收藏
页码:6 / 10
页数:5
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